Evidence map›Paper›PMID 20005050›Full record

ArticlePsychoneuroendocrinology2010

Prenatal thyroxine treatment disparately affects peripheral and amygdala thyroid hormone levels.

Pradeep K Shukla, Laura J Sittig, Brian M Andrus, Daniel J Schaffer, Kanchi K Batra, Eva E Redei

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  4. Review
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  12. Strain-specific vulnerability to alcohol exposure in utero via hippocampal parent-of-origin expression of deiodinase-III.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2011
    Article
  13. Candidate placental biomarkers for intrauterine alcohol exposure.Alcoholism, clinical and experimental research · 2011
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Pradeep K ShuklaDepartment of Psychiatry and Behavioral Sciences, The Asher Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Laura J Sittig
Brian M Andrus
Daniel J Schaffer
Kanchi K Batra
Eva E Redei
Northwestern University · US

Funding

Prenatal Alcohol;Hormone-Regulated Genes &BehaviorR01AA013452 · NIAAA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI REDEI, EVA E · 2002 to 2010
$2.3M
NIAAA NIH HHS AA013452NIAAA NIH HHS R01 AA013452
6 · The paper itself

Abstract

A prenatal hypothyroid state is associated with behavioral abnormalities in adulthood. Wistar Kyoto (WKY) rats exhibit hypothyroidism and increased depressive and anxiety-like behaviors. Thus, the WKY could illuminate the mechanisms by which the reversal of developmental hypothyroidism in humans and animals results in adult behavioral improvement. We examined the outcome of maternal thyroxine (T4) treatment on thyroid hormone-regulated functions and adult behavior of the WKY offspring. Pregnant WKY dams completed gestation with and without T4 administration and their adult male offspring were tested. Measures included depressive and anxiety-like behaviors, and thyroid hormone (TH) concentrations in both plasma and specific brain regions. In addition, the expression of two proteins affecting thyroid hormone trafficking and metabolism, monocarboxylate transporter 8 (MCT-8) and iodothyronine deiodinase type III (Dio3), and of several behavior-altering molecules, glucocorticoid receptor (GR), prepro-thyrotropin releasing hormone (prepro-TRH) and corticotrophin releasing hormone (CRH), were determined in the hippocampus and amygdala of the offspring. Prenatal T4 treatment of WKYs did not affect adult depressive behavior but increased anxiety-like behavior and decreased plasma levels of THs. In the hippocampus of males treated with T4 in utero, Dio3 and MCT-8 protein levels were increased, while in the amygdala, there were increases of free T4, MCT-8, GR, prepro-TRH protein and CRH mRNA levels. These results show that T4 administration in utero programs adult peripheral and amygdalar thyroid hormone levels divergently, and that the resulting upregulation of anxiety-related genes in the amygdala could be responsible for the exacerbated anxiety-like behavior seen in WKYs after prenatal T4 treatment.

Indexed as

AmygdalaAnimalsAnxietyCorticosteroneCorticotropin-Releasing HormoneDepressive DisorderDisease Models, AnimalFemaleHippocampusHypothyroidismIodide PeroxidaseMaleMonocarboxylic Acid TransportersPregnancyPrenatal Exposure Delayed EffectsProtein PrecursorsCorticosteroneCorticotropin-Releasing HormoneIodide Peroxidaseiodothyronine deiodinase type IIImonocarboxylate transporter 8, ratMonocarboxylic Acid Transportersprepro-thyrotropin-releasing hormoneProtein PrecursorsReceptors, GlucocorticoidThyrotropin-Releasing HormoneThyroxineTriiodothyronine

Identifiers

PMID20005050
PMCPMC2875313
OpenAlexW2142658622

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.